Carbonezi, Carlos Alberto [UNESP]Lopes, Márcia Nasser [UNESP]Silva, Dulce Helena Siqueira [UNESP]Araújo, Angela Regina [UNESP]Bolzani, Vanderlan da Silva [UNESP]Young, Maria Claudia MarxSilva, Marcelo Rogério da2014-05-202014-05-202004-04-01Química Nova. Sociedade Brasileira de Química, v. 27, n. 2, p. 196-198, 2004.0100-4042http://hdl.handle.net/11449/26276The bioactive compound trans-3'-methylsulphonylallyl trans-cinnamate (1) along with the inactives iryelliptin (2) and (7R,8S,1'S)-delta8'-3',5'-dimethoxy-1',4'-dihydro-4'-oxo-7.0.2',8.1'-neolignan (3) were isolated from the leaves of Cinnamomum australe. The structures of these compounds were assigned by analysis of 1D and 2D NMR data and comparison with data registered in the literature for these compounds. The DNA-damaging activity of 1 is being described for the first time.196-198porCinnamomum australeLauraceaeDNA-damaging activityDerivado cinamoílico com atividade no reparo de DNA e outras substâncias de Cinnamomum australe (Lauraceae)DNA-damaging activity of a cinnamate derivative and further compounds from Cinnamomum australe (Lauraceae)Artigo10.1590/S0100-40422004000200005S0100-40422004000200005Acesso abertoS0100-40422004000200005.pdf33101708996939444702004904231248003757905408316044840836852516730000-0001-7616-96520000-0002-1516-7765